Cruxi research & evidence
FDA 510(k) Submission Services evidence guides — page 69
Compare documented facts, dated analyses and evidence that can change your project scope. Confirm applicability with a specialist.
Compare FDA 510(k) Submission Services providers- Electric Breast Pump (HL-3058, F5112) (K252629): indications, design and recorded evidenceRegulatory decision evidence
- Electric Breast Pump (HL-3060, F5113) (K252630): indications, design and recorded evidenceRegulatory decision evidence
- Electric Breast Pump (K212564): indications, design and recorded evidenceRegulatory decision evidence
- Electric Breast Pump (YM-8807, YM-8805, YM-8806, YM-8810) (K252342): indications, design and recorded evidenceRegulatory decision evidence
- Electric Nasal Aspirator (BC026, BC025, BC023) (K250697): indications, design and recorded evidenceRegulatory decision evidence
- Electrical Stimulator - Model R-C1 TENS and EMS stimulator, Model R-E1 EMS stimulator, Model R-T1 TENS Stimulator (K180956): indications, design and recorded evidenceRegulatory decision evidence
- Electrocardiograph (K212278): indications, design and recorded evidenceRegulatory decision evidence
- Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder (QGH) — FDA decisions, comparisons and evidenceFDA record research
- Electrode, Electrosurgical, Active, Urological, Reprocessed (NLW) — FDA decisions, comparisons and evidenceFDA record research
- Electrode, Pacing And Cardioversion, Temporary, Epicardial (NHW) — FDA decisions, comparisons and evidenceFDA record research
- Electromagnetic Stimulator For Healthy Muscle Stimulation (SGT) — FDA decisions, comparisons and evidenceFDA record research
- Electromechanical Arm For A Transcranial Magnetic Stimulation System (QFF) — FDA decisions, comparisons and evidenceFDA record research
- Electronic Apex Locator (Alpha Apex I) (K242765): indications, design and recorded evidenceRegulatory decision evidence
- Electronic Blood Pressure Monitor (K232814): indications, design and recorded evidenceRegulatory decision evidence
- Electronic Peak Flow Meter (K230423): indications, design and recorded evidenceRegulatory decision evidence
- Electronic Stethoscope DS301 (K160023): indications, design and recorded evidenceRegulatory decision evidence
- Electrosurgical Patient Return Electrode (ODR) — FDA decisions, comparisons and evidenceFDA record research
- Electrosurgical, Cutting & Coagulation & Accessories (GEI) — FDA decisions, comparisons and evidenceFDA record research
- Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed (NUJ) — FDA decisions, comparisons and evidenceFDA record research
- Elegance® Anterior Cervical plate (K243904): indications, design and recorded evidenceRegulatory decision evidence
- Elemental Granulate (K241283): indications, design and recorded evidenceRegulatory decision evidence
- Elevator, Wheelchair, Portable (ING) — FDA decisions, comparisons and evidenceFDA record research
- Elfor-L (K243852): indications, design and recorded evidenceRegulatory decision evidence
- EliA B2-Glycoprotein I IgA Immunoassay, EliA Cardiolipin IgA Immunoassay (K181329): indications, design and recorded evidenceRegulatory decision evidence
- EliA Celikey IgG Immunoassay; EliA GliadinDP IgA Immunoassay; EliA GliadinDP IgG Immunoassay (K181871): indications, design and recorded evidenceRegulatory decision evidence
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